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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
8
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pubmed:dateCreated |
2004-8-6
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pubmed:abstractText |
The tumor necrosis factor (TNF) superfamily member LIGHT, which binds herpes virus entry mediator (HVEM) and lymphotoxin beta receptor (LTbetaR), plays important roles in regulating the immune response. To clarify the mechanism underlying graft arterial disease (GAD), we investigated the role of the LIGHT pathway in the progression of GAD.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-6,
http://linkedlifedata.com/resource/pubmed/chemical/LTBR protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Ltbr protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Lymphotoxin beta Receptor,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor...,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Virus,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/TNFRSF14 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/TNFSF14 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Tnfrsf14 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Tnfsf14 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor Ligand...,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1524-4636
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1409-15
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:15178556-Animals,
pubmed-meshheading:15178556-Aorta, Thoracic,
pubmed-meshheading:15178556-Cell Division,
pubmed-meshheading:15178556-Coculture Techniques,
pubmed-meshheading:15178556-Coronary Vessels,
pubmed-meshheading:15178556-DNA, Complementary,
pubmed-meshheading:15178556-Disease Progression,
pubmed-meshheading:15178556-Graft Rejection,
pubmed-meshheading:15178556-Heart Transplantation,
pubmed-meshheading:15178556-Humans,
pubmed-meshheading:15178556-Immunoglobulin G,
pubmed-meshheading:15178556-Interferon-gamma,
pubmed-meshheading:15178556-Interleukin-4,
pubmed-meshheading:15178556-Interleukin-6,
pubmed-meshheading:15178556-Lymphocyte Activation,
pubmed-meshheading:15178556-Lymphotoxin beta Receptor,
pubmed-meshheading:15178556-Membrane Proteins,
pubmed-meshheading:15178556-Mice,
pubmed-meshheading:15178556-Mice, Inbred BALB C,
pubmed-meshheading:15178556-Mice, Inbred C57BL,
pubmed-meshheading:15178556-Mice, Inbred Strains,
pubmed-meshheading:15178556-Muscle, Smooth, Vascular,
pubmed-meshheading:15178556-Myocytes, Smooth Muscle,
pubmed-meshheading:15178556-RNA, Messenger,
pubmed-meshheading:15178556-Receptors, Tumor Necrosis Factor,
pubmed-meshheading:15178556-Receptors, Tumor Necrosis Factor, Member 14,
pubmed-meshheading:15178556-Receptors, Virus,
pubmed-meshheading:15178556-Recombinant Fusion Proteins,
pubmed-meshheading:15178556-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:15178556-Transplantation, Heterotopic,
pubmed-meshheading:15178556-Transplantation, Homologous,
pubmed-meshheading:15178556-Tumor Necrosis Factor Ligand Superfamily Member 14,
pubmed-meshheading:15178556-Tumor Necrosis Factor-alpha
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pubmed:year |
2004
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pubmed:articleTitle |
Attenuation of graft arterial disease by manipulation of the LIGHT pathway.
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pubmed:affiliation |
Department of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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